67146-05-8

Basic information

• Product Name: sorbinil
• CAS NO: 67146-05-8
• Molecular Weight: 236.202
• Mol File: 67146-05-8.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: sorbinil(CAS DataBase Reference)
• NIST Chemistry Reference: sorbinil(67146-05-8)
• EPA Substance Registry System: sorbinil(67146-05-8)

Safety Data

• Hazardous Substances Data: 67146-05-8(Hazardous Substances Data)

Upstream product

• 371-41-5 4-Fluorophenol 
• 103834-11-3 (S)-4-amino-6-fluoro-chromane-4-carboxylic acid 
• 79791-46-1 (S)-4-cyano-2,3-dihydro-6-fluoro-4-<(S)-(1-phenylethyl)amino>-4H-1-benzopyran 
• 79791-44-9 (S)-2,3-dihydro-6-fluoro-4-<(1-phenylethyl)imino>-4H-1-benzopyran 
• 82799-12-0 (S)-1'-chloro-6-fluoro-2,3-dihydro-5'-imino-3'-<(S)-1-phenylethyl>spiro<4H-1-benzopyran-4,4'-imidazolidin>-2'-one hydrochloride 
• 103197-13-3 (S)-methyl 4-amino-6-fluorochroman-4-carboxylate 
• 103197-09-7 4-amino-2,3-dihydro-6-fluoro-4H-1-benzopyran-4-carboxylic acid, hydrochloride 
• 103197-05-3 N-acetyl-2-(2-bromoethoxy)-5-fluorophenylglycine 
• 103197-08-6 4-acetamido-2,3-dihydro-6-fluoro-4H-1-benzopyran-4-carboxylic acid 
• 103196-96-9 C₁₂H₁₀FNO₃ 
• 332-48-9 2-(4-fluorophenoxy)-ethylbromide 
• 85169-02-4 3-(4-fluoro-phenoxy)propionitrile 
• 66892-34-0 6-fluoro-4-chromanone 
• 1579-78-8 3-(4-fluoro-phenoxy)propionic acid 

Relevant articles and documents

USE OF SUBSTITUTED 2 PHENYLBENZIMIDAZOLES AS MEDICAMENTS

The present invention relates to the use of a substituted 2-phenylbenzimidazole of formula I wherein R1, R2, R3, R 4, R5 and m have the meanings given in the claims, for the preparation of a medicament for the treatment or prevention of diseases involving glucagon receptors, as well as new compounds of formula I wherein R1 is a group of formula

Lipase-catalyzed resolution of 5,5-disubstituted hydantoins

Chiral non-racemic 5,5-disubstituted hydantoins were prepared by lipase-catalyzed enantioselective hydrolyses of their N-acyloxymethyl groups or esterification of their N-hydroxymethyl groups.

Novel synthesis of the aldose reductase inhibitor sorbinil via amidoalkylation, intramolecular oxazolidin-5-one alkylation, and chymotrypsin resolution

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